NCT02820220

Brief Summary

Observational, cross sectional study, carried out with the help of a pre-designed and pre-tested questionnaire with the research hypothesis as: Knowledge and perception regarding JSSK and RBSK in nursing students is better as compared to in-service nurses as well as patients/patient attendants (attending LHMC and associated hospitals, New Delhi, India)

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
293

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2015

Shorter than P25 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2015

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2016

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

June 24, 2016

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 30, 2016

Completed
Last Updated

June 30, 2016

Status Verified

June 1, 2016

Enrollment Period

1 year

First QC Date

June 24, 2016

Last Update Submit

June 29, 2016

Conditions

Keywords

KnowledgeProgramsPatientsStudentsNurses

Outcome Measures

Primary Outcomes (1)

  • Knowledge and perception regarding JSSK and RBSK in study population groups

    The knowledge and perception will be evaluated by yes, no responses using predesigned and pretested questionnaire presented to each of the three study groups.

    90 days

Secondary Outcomes (2)

  • Comparison of the knowledge and perception regarding JSSK and RBSK in study population groups

    90 days

  • Study of factors contributing to knowledge regarding JSSK and RBSK in study population groups

    90 days

Study Arms (3)

Patient/patient attendants

1. Study subjects will be females. 2. Age at enrolment should be more than 18 years. 3. Attending Department of Paediatrics OPD/emergency/well-baby clinics/immunisation clinics OR Department of Gynaecology and Obstetrics OPD/emergency/Ante-natal clinics/Post-natal clinics of Lady Hardinge Medical College and associated hospitals. 4. Written informed consent to participate in the study.

Students,nursing

1. Pursuing Bsc Nursing(in their final year) or intern of college of nursing LHMC 2. Written informed consent to participate in the study

In-service nurses

1. Posted in Department of Paediatrics indoor/OPD/well-baby clinics/immunisation clinics or Department of Gynaecology and Obstetrics indoor/OPD/emergency/Ante-natal clinics/Post-natal clinics of Lady Hardinge Medical College and associated hospitals. 2. Written informed consent to participate in the study.

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

100 participants enrolled from the patients/attendant subset,93 Nursing students(final year) and interns from the Nursing college, LHMC along with 100 nurses posted in the LHMC and associated hospitals enrolled in the study.

You may qualify if:

  • Group 1) Patients/Attendants:
  • All study subjects must be female.
  • Age more than 18 years.
  • Written informed consent to participate in the study.
  • Group 2) Nursing Student:
  • Students / intern at College of nursing LHMC pursuing Bsc Nursing
  • Written informed consent to participate in the study
  • Group 3) In-service Nurses:
  • Posted in Department of Paediatrics indoor/OPD/well-baby clinics/immunisation clinics or Department of Gynaecology and Obstetrics indoor/OPD/emergency/Ante-natal clinics/Post-natal clinics of Lady Hardinge Medical College and associated hospitals.
  • Written informed consent to participate in the study

You may not qualify if:

  • Males for the patient/attendant group 1

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Vikram Datta, MD,DNB

    Lady Hardinge Medical College,New Delhi,India

    STUDY CHAIR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

June 24, 2016

First Posted

June 30, 2016

Study Start

June 1, 2015

Primary Completion

June 1, 2016

Study Completion

June 1, 2016

Last Updated

June 30, 2016

Record last verified: 2016-06